2010
DOI: 10.1093/qjmed/hcq194
|View full text |Cite
|
Sign up to set email alerts
|

Neurosarcoidosis: rare initial presentation with seizures and delirium

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
4
1

Citation Types

0
6
0

Year Published

2013
2013
2019
2019

Publication Types

Select...
5
1

Relationship

0
6

Authors

Journals

citations
Cited by 7 publications
(6 citation statements)
references
References 5 publications
0
6
0
Order By: Relevance
“…In some pathophysiologically disturbed cases, we observe neuropsychiatric symptoms such as epileptic seizure and delirium [19, 20]. Several studies have shown that epilepsy occurs in line with autonomic imbalance, an increased sympathetic activity and a reduced parasympathetic activation [21, 22].…”
Section: Discussionmentioning
confidence: 99%
“…In some pathophysiologically disturbed cases, we observe neuropsychiatric symptoms such as epileptic seizure and delirium [19, 20]. Several studies have shown that epilepsy occurs in line with autonomic imbalance, an increased sympathetic activity and a reduced parasympathetic activation [21, 22].…”
Section: Discussionmentioning
confidence: 99%
“…5,19 The CSF may present hyperproteinemia in 73% of the patients and lymphocytosis in 55%; normal CSF is uncommon. 2,5,11 The non-caseating granuloma of sarcoidosis has immunological origin, and is formed by giant cells and epithelioid cells (consisting of histiocytes modified by T lymphocytes). The presence of giant and epithelioid cells is a sign of high cellular turnover.…”
Section: Discussionmentioning
confidence: 99%
“…4 The clinical presentation of neurosarcoidosis is usually optic neuropathy, facial paralysis, meningitis, chronic meningitis, diabetes insipidus, hydrocephalus, elevated intracranial pressure, spinal cord syndromes, vasculitis, cerebral infarction, dysfunctional hypothalamus, myelopathy, myopathy, peripheral neuropathy, and encephalitis (►Table 1); the presentation of psychiatric symptoms and osseous involvement is rare. 3,[10][11][12][13][14] Cranial nerve alteration is present in 50-75% of the patients with neurosarcoidosis, and the most common affected nerves are, in descending order, cranial nerves VII, II and VIII. Cranial nerve VII is unilaterally affected in 65% of the cases, and bilaterally affected in 35%; 7,15 cranial nerve II is affected in 5-25% of the patients.…”
Section: Clinical Manifestationsmentioning
confidence: 99%
“…These symptoms are observed in NS (8,9). NS tends to have a poor outcome if presented with epileptic seizures initially (5,10). In spinal cord involvement of sarcoidosis, para/tetra paresis, autonomic dysreflexia, radicular syndrome, or cauda equine syndrome can be observed because of transverse myelopathy (11,12,13,14,15).…”
Section: Discussionmentioning
confidence: 99%
“…Along with the detection of nonspecific findings, such as protein increase, the levels of leukocytosis or pleocytosis, ACE (21,22), immune globulin G index, CD4:CD8 lymphocyte ratio (23), an increase of beta 2-microglobulin, and the positivity of oligoclonal band (OCB) in CSF provides important clues for NS diagnosis. However, CSF examination can be normal in NS cases (5,18,24). In 6 of our cases, an increment in protein and ACE levels was detected in CSF examinations; pattern III OCB positivity in one case and pattern IV OCB positivity in one case were observed.…”
Section: Discussionmentioning
confidence: 99%